Hi Rams,

Given the ligand is identical in all structures I'd create and object from just 
the ligand and then write a script to align all 50 structures with that ligand 
object. I've done that on number of cases.

Hope it works in your case as well.

Vaheh

From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> On Behalf Of Subramanian, 
Ramaswamy
Sent: Saturday, July 15, 2023 8:10 AM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Ligand superposition!

Thanks Boaz,

The proteins are all completely different in folds and structures!


Rams
subra...@purdue.edu<mailto:subra...@purdue.edu>




On Jul 15, 2023, at 8:04 AM, Boaz Shaanan 
<bshaa...@bgu.ac.il<mailto:bshaa...@bgu.ac.il>> wrote:

---- External Email: Use caution with attachments, links, or sharing data ----

Hi,
-You may want to send a query to the UCSF chimerax/chimera people. They may 
suggest how to this using scripts.
- I have not done this on 50 structures, only on few ones. In my experience, if 
the proteins are sufficiently similar there is a good chance that superimposing 
the proteins will also bring the ligands to near superposition.
-Using chimera/chimerax you can select protein residues within certain radius 
from the ligands, write out the pdb's and then perhaps superimpose those 
smaller pdb's. I have not tried this.
Sorry I can't be of more help.
Cheers,
Boaz



Boaz Shaanan, Ph.D.
Dept. of Life Sciences
Ben-Gurion University of the Negev
Beer-Sheva 84105
Israel

E-mail: bshaa...@bgu.ac.il<mailto:bshaa...@bgu.ac.il>
Phone: 972-8-647-2220
Fax:   972-8-647-2992 or 972-8-646-1710




________________________________
From: CCP4 bulletin board on behalf of Subramanian, Ramaswamy
Sent: Friday, July 14, 2023 10:49 PM
To: CCP4BB@JISCMAIL.AC.UK<mailto:CCP4BB@JISCMAIL.AC.UK>
Subject: [ccp4bb] Ligand superposition!

Hi All,

I have over 50 pdb files that I have downloaded from PDB that all have the same 
ligand bound.

I wamt to superpose the ligands (and move the protein coordinates using that 
matrix).  The goal is for me to see how difference in ligand environments in 
different complexes.

Is there an easy way to do it?  I am sure it has been done before and I do not 
want to reinvent the wheel.

Thanks.



Rams
subra...@purdue.edu<mailto:subra...@purdue.edu>



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